The Lumbar Region

CHAPTER 7 The Lumbar Region




The lumbar portion of the vertebral column has the ideal structure to simultaneously optimize the functions of mobility and stability (Putz and Müller-Gerbl, 1996). This region of the spine is sturdy and is designed to carry the weight of the head, neck, trunk, and upper extremities. However, pain in the lumbar region is one of the most common complaints of individuals, experienced by approximately 80% of the population at some time in their lives (Nachemson, 1976; Jonsson, 2000). The estimated annual cost for low back pain claims in the U.S. in 1995 was $8.8 billion (Borenstein, 2000) and is undoubtedly greater than that today. The total annual costs of treatment, loss of productivity, and resulting disability are estimated to be more than $28 billion in the United States (Rizzo, Abbott, and Berger, 1998). Low back pain is the most common complaint of patients who go to clinics that deal primarily with musculoskeletal conditions. Low back pain of mechanical origin is the most frequent subtype found in this group (Cramer et al., 1992a). The most common sources of low back pain are the lumbar zygapophysial joints (Z joints) and intervertebral discs (IVDs) (Bogduk, 1985).


Much of the reason for the high incidence of low back pain is probably related to humans being bipedal. Being able to walk on the hind limbs is accompanied by increased freedom of movement and increased ability to interact with the environment, other species, and other members of the same species. Animals that walk on the hind legs (primarily humans) can normally turn their heads with relative ease to look around to both the left and right sides. They also have the ability to use their hands for an almost infinite number of tasks without having to be concerned about using their upper extremities to help maintain balance.


However, the ability to walk on the lower extremities (the bipedal stance) has one significant drawback: Increased stress is placed on the spine. The weight of the body is concentrated on a smaller region compared with quadrupeds. The weight of the human trunk is completely supported by the lower extremities and lumbar spine during standing and it is completely absorbed by the lumbar spine and sacroiliac joints during sitting. Therefore the lumbar region, sacrum, and sacroiliac joints are susceptible to more problems than are encountered by four-legged animals. These problems can be divided into three types of lumbar disorders and sacroiliac joint difficulties:



1. Problems with the lumbar region
a. The Z joints (facet joints; see Figs. 7-3 through 7-6). Increased weight borne by these joints can be a direct cause of back pain. These joints also are susceptible to arthritic changes (e.g., osteoarthritis; arthritis associated with wear and tear).

b. The intervertebral disc. The IVDs absorb most of the increased stress received by the low back in bipeds. The discs may bulge or protrude, and by doing so compress the spinal nerves that exit behind them (see Figs. 7-24, 7-25, 11-10, and 11-11). Such protrusion can result in back pain that also has a sharp radiation pattern into the thigh and sometimes into the leg and foot. This type of pain is frequently described as feeling like a “bolt of lightning” or a “hot poker” (see Chapter 11). The IVDs may undergo degeneration also. This narrows the space between the vertebrae, which may result in arthritic changes and additional pressure on the Z joints (see Chapters 2 and 14). The discs themselves are supplied by sensory nerves and therefore can be a direct source of back pain (i.e., they do not have to compress neural elements to cause back pain).

c. The muscles of the low back in bipeds are called on to hold the spine erect (erector spinae muscles; see Chapter 4). Therefore when they are required to carry increased loads (this sometimes includes the added weight of a protruding abdomen), these muscles can be torn (strained).

image

FIG. 7-4 Orientation of lumbar Z joints. Notice the changes from L1-2 to L5-S1.


(From Taylor JR & Twomey LT. (1986). Age changes in lumbar zygapophyseal joints: Observations on structure and function. Spine, 11, 739-745.)






Note: The lumbosacral region, between L5 and the sacrum, receives the brunt of the biomechanical stress of the biped spine. The lumbosacral joints (interbody joint and left and right Z joints between L5 and the sacrum) are a prime source of low back pain. In addition to the biomechanical stresses, the opening for the spinal nerve at this level is the smallest in the lumbar region, making it particularly vulnerable to IVD protrusions and compression from other sources.



The lumbar region has been the focus of extensive high-quality research because of its clinical importance. Numerous descriptive, quantitative, and experimental studies have been completed on this area of the spine. This chapter concentrates on the unique characteristics of the lumbar vertebrae and the ligamentous, neural, and vascular elements of the lumbar region. It also includes the most pertinent results of research in an attempt to explain clearly the most important and clinically relevant idiosyncrasies of this intriguing area of the spine.


All the lumbar vertebrae are considered to be typical, although the fifth lumbar vertebra is unique. This chapter presents the typical characteristics of lumbar vertebrae, the lumbar vertebral canal, and the intervertebral foramina (IVFs). A description of the unique characteristics of L5 and the lumbosacral articulation follows. The ranges of motion of the lumbar region are included also. The chapter concludes with a discussion of the nerves, vessels, and related viscera of the lumbar region.



LUMBAR LORDOSIS AND CHARACTERISTICS OF TYPICAL LUMBAR VERTEBRAE



Developmental Considerations and the Lumbar Curve (Lordosis)


The development of lumbar vertebrae is similar to the development of typical vertebrae in other regions of the spine (see Chapter 12). Two additional secondary centers of ossification on each vertebra are unique to the lumbar region. This brings the total number of secondary centers of ossification per lumbar vertebra to seven. These additional centers are located on the posterior aspect of the superior articular processes and develop into the mamillary processes.


Between 2 and 16 years of age, the lumbar vertebrae grow twice as fast as the thoracic vertebrae. Because the anteroposterior curves of these two regions face in opposite directions (thoracic kyphosis versus lumbar lordosis), the posterior elements of thoracic vertebrae probably grow faster than their vertebral bodies; the reverse (lumbar vertebral bodies grow faster than their posterior elements) is true in the lumbar region (Clarke et al., 1985).


Normally the lumbar lordosis is more prominent than the cervical lordosis. The lumbar lordosis extends from T12 to the L5 IVD, and the greatest portion of the curve occurs between L3 and L5 (Fig. 7-1). The lumbar lordosis is created by the increased height of the anterior aspect of both the lumbar vertebral bodies and the lumbar IVDs, with the discs contributing more to the lordosis than the increased height of the vertebral bodies.



Either an increase or decrease of the lumbar lordosis may contribute to low back pain (Mosner et al., 1989). This has sparked an interest in measurement of the lumbar curve; as a result, the lumbar curve has been measured in a variety of ways. One method, developed by Mosner et al. (1989), used measurements from lateral x-ray films taken with the patient in the supine position. A line was drawn across the superior vertebral end plate of L2 and another across the superior aspect of the sacral body. These two lines were continued posteriorly until they intersected, and the angle between them was measured. Using this method, an angle of 47 and 43 degrees was found to be normal for women and men, respectively. This is in agreement with the values given by other authors (Williams et al., 1995).


Another relatively common method of measuring the lumbar lordosis calls for passing a line across the superior aspect of the body of L1 and another such line across the body of the first sacral segment, and then measuring the angle formed by the intersection of the continuation of the two lines. However, care must be taken when making such measurements. Normally the first lumbar vertebral body is slightly taller anteriorly than posteriorly; however, a relatively frequent anomaly is for the first lumbar vertebral body to be wedge shaped, so that it is shorter anteriorly than posteriorly. Such wedging of the vertebra being used as a landmark for measurement can cause significant variation of measurements of the lumbar lordosis (Worril and Peterson, 1997).


In the past, many clinicians incorrectly assumed that the lumbar lordosis in the black population was greater than that in the white population, but this has been found to be incorrect; the lordosis is appromimately the same in both races (Mosner et al., 1989).




Vertebral Bodies


When viewed from above, the vertebral bodies of the lumbar spine are large and kidney shaped with the concavity facing posteriorly (Fig. 7-2). However, L5 is more elliptical in shape. In addition, the inferior and superior bony end plates of adjacent vertebrae sharing the same IVD are similar in size and shape. Although the lumbar vertebral bodies of males generally have greater dimensions than those of females, the shapes of the vertebral bodies are similar (Hall et al., 1998). The superior surfaces of the vertebral bodies possess small elevations along their posterior rim. These represent remnants of the uncinate processes of the cervical region. The inferior surfaces of the vertebral bodies have two small notches along their posterior rim. These notches correspond to the uncinate-like elevations of the vertebra below. These elevations and notches have been used as landmarks on x-ray films as a means for evaluating normal and abnormal movement between adjacent lumbar segments (Dupuis et al., 1985).



The vertebral bodies are wider from side to side (lateral width) than from front to back and are taller in front (anteriorly) than behind. Therefore as mentioned, the vertebral bodies are partially responsible for the creation and maintenance of the lumbar lordosis.


Normally the lateral width of the lumbar vertebrae increases from L1 to L3. L4 and L5 are somewhat variable in width (Williams et al., 1995). Ericksen (1976, 1978) found that the L1-4 vertebral bodies (he did not study L5) became wider from side to side with age. Also, he noted a decrease in height of the vertebral body’s anterior aspect, corresponding with an increase in its lateral width, in both males and females. Further, the increase in lateral width in males was accompanied by a corresponding decrease in height of the vertebral body’s posterior aspect (Erickson, 1976, 1978).


Up to 90% of the compressive loads received by the vertebral bodies are carried by the inner cancellous (trabecular) bone (Silva, Keaveny, and Hayes, 1997); however, this may be an overestimation (Cao, Grimm, and Yang, 2001). The remaining 10% (or more) of the compressive loads are carried by the thin outer cortical shell of the vertebral bodies (Silva, Keaveny, and Hayes, 1997). However, with the bone loss associated with osteoporosis a higher percentage of the compressive loads are carried by the outer extra cortical shell of bone (Cao, Grimm, and Yang, 2001).


Perhaps somewhat paradoxically, the bony end plates of the vertebral bodies are particularly important in resisting compressive loads placed on the spine. Oxland et al. (2003) found that removal of the bony end plates decreased the ability of the vertebral bodies to resist compression fracture by 66%. The end plates of the lumbar region are weakest in the center, and strongest posterolaterally. In addition, the inferior end plates are stronger than the superior ones, and the sacral end plate is similar in strength to the inferior lumbar bony end plates (Grant, Oxland, and Dvorak, 2001).


The blood supply to the lumbar vertebral bodies is extensive and complex (Bogduk, 1997). Each lumbar segmental artery gives off up to 20 primary periosteal arteries as it courses across the anterolateral aspect of the vertebral body. The posterior aspect is supplied by many branches of the anterior vertebral canal artery. The anterior vertebral canal artery refers to the anterior branch of the artery that passes through the IVF. The artery that passes through the IVF sometimes is known as the spinal ramus of the (lumbar) segmental artery.


The end branches of periosteal arteries form a ring around both the superior and inferior margins of the vertebral body. These rings are known as the metaphyseal anastomoses (superior and inferior). They not only help to supply the metaphyseal region of the vertebral body, but also send penetrating branches (metaphyseal arteries) to the region of the vertebral end plate (Bogduk, 1997). A dense capillary network is associated with the superior and inferior vertebral end plates. This network receives contributions from the metaphyseal and nutrient arteries.


Nutrient arteries also arise from the anterior vertebral canal arteries. The nutrient arteries enter the center of the posterior aspect of the vertebral body, pass deep within the substance of the cancellous bone of the vertebral body’s center, and then give off superior (ascending) and inferior (descending) branches. In addition to giving off periosteal arteries, the lumbar segmental arteries also send branches that enter the cancellous bone of the anterior and lateral aspects of the vertebral bodies. These branches enter along the superior-to-inferior midpoint of the vertebral bodies. Known as the equatorial arteries, these vessels are similar to the nutrient arteries in that they also give rise to ascending and descending branches deep within the substance of the vertebral bodies (Bogduk, 1997). See Chapter 2 and Figure 2-3 for further details on the blood supply to and venous drainage of typical vertebrae.


The lumbar vertebral bodies serve as attachment sites for several structures. Table 7-1 lists those structures that attach to the lumbar vertebral bodies.


Table 7-1 Attachments to Lumbar Vertebral Bodies















Region Structure(s) Attached
Anterior surface Anterior longitudinal ligament on superior and inferior borders
Posterior surface Posterior longitudinal ligament on superior and inferior borders
Lateral surface


From Williams PL et al. (1995). Gray’s anatomy (38th ed.). Edinburgh: Churchill Livingstone.





Transverse Processes


Each transverse process (TP) (left and right) of a typical lumbar vertebra projects posterolaterally from the junction of the pedicle and the lamina of the same side (see Fig. 7-2). It lies in front of (anterior to) the articular processes and behind (posterior to) the lumbar IVF.


The lumbar TPs are quite long, the TPs of L3 being the longest. The distance between the apices of the left and right TPs is much greater on L1 than T12. This distance increases on L2 and is the greatest in the entire spine on L3. The intertransverse distance between the left and right L4 TPs is smaller than that of L3 and is even smaller for L5. The lumbar TPs are flat and thin from front to back. They are also narrower from superior to inferior than their thoracic counterparts. They possess neither articular facets (as do thoracic TPs) nor foramina of the transverse processes (as do cervical TPs). The anterior aspect of the lumbar TPs also are known as the costal elements, and they occasionally develop into ribs. This happens most frequently at L1.


The lateral aspect of the anterior surface of the lumbar TPs is creased by a ridge that runs from superior to inferior. This ridge is created by the anterior layer of the thoracolumbar fascia. The middle layer of the thoracolumbar fascia attaches to the apex of the TPs. Table 7-2 lists structures that attach to the lumbar TPs.


Table 7-2 Attachments to Lumbar Transverse Processes





















Region Structure(s) Attached
Anterior surface


Apex Middle layer of thoracolumbar fascia Iliolumbar ligament (L5, occasionally L4)
Superior border Lateral intertransversarius muscle
Inferior border Lateral intertransversarius muscle
Posterior surface Deep back muscles (longissimus thoracis)

From Williams PL et al. (1995). Gray’s anatomy (38th ed.). Edinburgh: Churchill Livingstone.




Articular Processes



Superior Articular Processes.


Left and right superior articular processes are formed on every vertebrae of the lumbar spine (see Fig. 7-2). Each superior articular process possesses a hyaline cartilage–lined superior articular facet that is oriented in a vertical plane. That is, these facets are not angled to the vertical plane like the superior articular facets of the cervical and thoracic regions.


All the lumbar superior articular facets face posteriorly and medially. The articular surface of a typical superior articular facet can be gently curved with the concavity facing medially (Figs. 7-3 and 7-4), or the articular surface can be angled abruptly. When the articular surface is angled abruptly, two relatively distinct articulating surfaces are formed. One surface faces posteriorly and forms almost a 90-degree angle with the second surface, which faces medially. As with the curved facet, the concavity faces posteriorly and medially. In either case (curved or angled articular surface), the shape conforms almost perfectly to the inferior articular facet of the vertebra above. The hyaline cartilage of the central region of the superior articular facet (the area of greatest concavity) increases in thickness with age, probably because this region receives much of the load during flexion of the spine (Taylor and Twomey, 1986). Also, the articular processes may fracture as a result of age-related degeneration (Kirkaldy-Willis et al., 1978).


The orientation of the superior articular facets varies from one vertebral level to another (see Fig. 7-4). A line passed across each superior articular facet, on transverse CT scans, shows that the L4 superior facets (and therefore the L3-4 Z joints) are more sagittally oriented than the L5 facets. Also, the S1 superior facets (and therefore the L5-S1 Z joints) are more coronally oriented than the L4 and L5 facets (Van Schaik, Verbiest, and Van Schaik, 1985). (See Zygapophysial Joints for further detail on the orientation of the superior and inferior articular facets.)


The mamillary processes (see Fig. 7-2), which project posteriorly from the superior articular processes of lumbar vertebrae, are unique to the lumbar spine. Each mamillary process is a small rounded mound of variable size. Some are almost indistinguishable, whereas others are relatively prominent. The mamillary processes serve as attachment sites for the multifidi lumborum muscles.



Mamillo-Accessory Ligament.


A mamillo-accessory ligament (Bogduk, 1981; Lippitt, 1984) is found between the mamillary and accessory processes on the left and right sides of each lumbar vertebra. Occasionally one or more of these ligaments may ossify in the lower lumbar levels (L3-5). The incidence of ossification increases in frequency from L3 to L5. Ossification of these ligaments at L5 occurs at a frequency of 10% (Bogduk, 1981) to 26% (Maigne, Maigne, and Guervin-Surville, 1991). Maigne, Maigne, and Guervin-Surville (1991) studied 203 lumbar spines and found that ossification of this ligament at L5 occurred twice as often on the left. They gave no reason why the ligament ossified more frequently on this side. However, they believed the ossification was the result of osteoarthritis, because they found no evidence of ossification on the spines of children and young adults. These authors also stated that an ossified mamillo-accessory ligament could occasionally be seen on standard lumbar x-ray films.


The mamillo-accessory ligament has been described as a tough, fibrous band that may represent tendinous fibers of origin of the lumbar multifidi muscles or fibers of insertion of the longissimus thoracis pars lumborum muscle (Bogduk, 1981). Regardless of its precise structure, the reported purpose of the mamillo-accessory “ligament” is to hold the medial branch of the dorsal ramus of the above spinal nerve (e.g., the L2 medial branch is associated with the L3 mamillo-accessory ligament) against (a) the bone between the base of the superior articular process and the base of the transverse process, and (b) the Z joint, which is slightly more medial (Fig. 7-5). The medial branch of the dorsal ramus gives off articular branches to the capsule of the Z joint as it passes deep to the mamillo-accessory ligament. The medial branch then continues medially across the vertebral lamina to reach the multifidus muscle (Bogduk, 1981). Therefore the medial branch of the dorsal ramus (posterior primary division) is held within a small osteofibrous canal along the posterior arch of a lumbar vertebra. The medial branch could possibly become irritated or even entrapped within this tunnel, which would result in low back pain. However, more investigation is necessary to determine if such irritation or entrapment occurs and, if so, its frequency (Bogduk, 1981; Maigne, Maigne, and Guerin-Surville, 1991).




Zygapophysial Joints



General Considerations.


The Z joints have been positively identified as a source of back pain (Mooney and Robertson, 1976; Yamashita et al., 1990; Bogduk, 1992; Dreyfuss and Dreyer, 2001). In addition, Rauschning (1987) states that these joints “display typical degenerative and reparative changes which are known to cause osteoarthritic pain in peripheral synovial joints.” Thereore the lumbar Z joints are highly significant clinically. Because these joints are discussed in detail in Chapter 2, this section focuses on the unique and clinically significant aspects of the lumbar Z joints.


The lumbar Z joints are considered to be complex synovial joints oriented in the vertical plane (Williams et al., 1995). They are fashioned according to the shape of the superior and inferior articular facets (see previous discussion). Therefore the lumbar Z joints are concave posteriorly and even have been described as being biplanar in orientation (Taylor and Twomey, 1986). That is, they have a coronally oriented, posterior-facing, anteromedial component and a large, sagittally oriented, medial-facing, posterolateral component. Taylor and Twomey (1986) state that the lumbar Z joints are coronally oriented in children and that the large sagittal component develops as the individual matures. The sagittal component limits rotation, whereas the coronal component limits flexion. More specifically, the shape of the lumbar Z joints allows a large amount of flexion to occur in the lumbar region, yet the size of the lumbar Z joints is what eventually limits flexion at the end of the normal range of motion. Therefore the long contact surfaces between the coronal component of the superior articular processes and the adjacent inferior articular processes finally limit flexion by “restraining the forward translational component of flexion” (Taylor and Twomey, 1986).


Even though the size of the Z joints eventually limits flexion, approximately 60 degrees of flexion is able to occur in the lumbar region before the bony restraints of the lumbar articular processes prevent further movement. However, the size and shape of the Z joints dramatically limit rotation. By limiting rotation, the Z joints protect the IVDs from rotational injury. During rotation of the lumbar region, distraction (or gapping) occurs between adjacent lumbar articular facets (superior facet of vertebra below and inferior facet of vertebra above) on the side of rotation. For example, right rotation results in gapping of the facets on the right side. Also during rotation, the two opposing facets of the opposite side are pressed together. This causes them to act as a fulcrum for the distracting facets on the side of rotation (Paris, 1983; Cramer et al., 2003). Side posture spinal adjusting, performed by chiropractors and other health practitioners, also causes gapping of the Z joints. The gapping action produced by such adjustive procedures is thought to break-up fibrous adhesions that develop in Z joints that are moving less than normal (are hypomobile) (Cramer et al., 2000, 2002, 2003).


Extension of the lumbar region is limited by the inferior articular process on each side of a lumbar vertebra contacting the junction between the lamina and superior articular process of the vertebra below. This junction between the lamina and superior articular process is known as the pars interarticularis.




Biomechanical Considerations.


The articular facets do not absorb any of the compressive forces of the spine when humans are sitting erect or standing in a slightly flexed posture. The IVD and vertebral bodies absorb almost all the compressive loads under these conditions. However, when standing erect (slight extension), the facets resist approximately 16% (range, 3% to 25%) of the compressive forces between vertebrae. Disc degeneration may lead to increased stress on the Z joints, causing them to resist up to approximately 47% of the loads. This results in pain, not from the articular cartilage, but usually from pressure on the subchondral bone of the articular processes, soft tissue being caught between the articular facets, or added strain on the articular capsules (Dunlop, Adams, and Hutton, 1984; Yang and King, 1984; Hutton, 1990). In addition, beyond the limit of normal physiologic flexion, the inferior articular process is forced over the superior articular process, and the compressive loads carried by the facets again increase from those carried in the neutral position (Shirazi-Adl and Drouin, 1987).


The superior and inferior articular processes of the Z joints also resist anterior shear forces. The articular processes carry approximately one third of the anterior shear forces during forward flexion, whereas the IVDs carry approximately two thirds of the shear loads (when the load is applied suddenly). However, because of the viscoelasticity of the IVD, if a shear load is applied slowly, the vertebra above creeps further forward than when shear loads are applied rapidly. Thus the shear forces on the articular processes are increased with slowly applied and long-lasting loads in forward flexion (e.g., bending forward for long periods to weed a garden).



Articular Capsules.


An articular capsule covers the posterior aspect of each lumbar Z joint (see Fig. 7-5), and the ligamentum flavum covers the anteromedial aspect of the Z joint. The articular capsule is tough, possesses a rich sensory innervation, and is well vascularized (Giles and Taylor, 1987; Ashton et al., 1992).


The bundles of collagen fibers that form the thick outer fibrous layer of a typical lumbar Z joint capsule are oriented in different directions, depending on whether the fibers are located in the superior, middle, or inferior aspect of the capsule. The superior fibers attached laterally to the groove that is located between the mamillary process and posterior ridge of the superior articular process. From here the fibers of the superior capsule course medially across the superior joint recess, attaching to the medial aspect of the laminae of the superior-most vertebrae forming the Z joint. Fibers of the middle part of the Z joint capsule course more horizontally (lateral to medial), beginning from their attachment to the posterior aspect of the mamillary process (on the posterior aspect of the superior articular process) (Yamashita et al., 1996). These fibers then cross the Z joint gap and attach to the medial part of the lamina of the suprajacent vertebra. The fibers just described extend a considerable distance medially and become continuous with the lateral fibers of the interspinous ligament. Finally, the fibers of the more inferior aspect of the capsule course from superomedial to inferolateral, covering the joint space and the inferior end of the inferior Z joint recess. The superomedial fibers attach to the medial and inferior part of the lamina. The bundles of collagen fibers of this inferior aspect of the capsule are longer and thicker than those of the superior aspect of the capsule (Yamashita et al., 1996).


The orientation of the fibers within the tough outer layer of the capsule helps to limit forward flexion (Paris, 1983). The medial to lateral arrangement of the fibers in the central part of the Z joint may tend to stabilize the joint during axial rotation, while allowing movement in flexion and extension (Yamashita et al., 1996). The contribution of the lumbar Z joint capsule to stabilize and perhaps even helping to limit motion during axial rotation also has been supported by biochemical studies that show evidence of increased capsular resistance to tension in regions of the capsule that would receive the greatest stretch during this motion (Boszczyk et al., 2001). The collagen fibers of the superior and middle aspects of the Z joint are shorter than those of the inferior aspect of the capsule and are thought to be under more tensile stretch than the inferior aspect of the capsule. The posterosuperomedial-most corner of capsule (just inferior to the superior Z joint recess) is thought to be the area of the capsule that receives the highest tensile stretch (Yamashita et al., 1996). In fact, Yamashita et al. (1996) stated that the lumbar Z joint capsules undergo “extensive stretch under physiological loads.”


The collagen fibers of the inferior aspect of the lumbar Z joint capsules are thicker and more heavily innervated than the superior and middle aspects of the capsules. This may be because the inferior aspects of the capsule can be compressed (therefore requiring increased thickness), and even pinched (thus resulting in pain from additional nociceptive nerve endings), during full extension of the lumbar region (Yamashita et al., 1996).


Laterally, fibers of each articular capsule frequently are continuous with the articular cartilage lining the superior articular facet. A gradual transition occurs from the fibrous tissue of the capsule to fibrocartilage and finally to the hyaline cartilage of the superior articular facet (Taylor and Twomey, 1986).


Each capsule has a relatively large superior and inferior recess that extends away from the joint. The capsular fibers (or fibers of the ligamentum flavum, anteriorly) surrounding these recesses are relatively thin and loose, and there may be openings through which neurovascular bundles enter the recesses (Taylor and Twomey, 1986). Paris (1983) states that effusion within the Z joint may enter the superior recess and as little as 0.5 ml of effusion may cause the superior recess to enter the anteriorly located IVF. Once in the IVF, this expanded superior capsular recess may compress the dorsal root ganglion or the exiting spinal nerve, resulting in radiculopathy (see Chapter 11 for a full discussion of radiculopathy). Such a distinct protrusion of the superior recess of the Z joint capsule constitutes an example of a large Z joint synovial cyst (Xu et al., 1991; Bougie, Franco, and Segil, 1996).


Xu et al. (1991), in a study of 50 pairs of lumbar Z joints from an elderly population, found that the capsules varied greatly in thickness and regularity. They found that the capsules were “irregularly thickened, amorphous, and calcified in 22 cases.” In addition, they found that in most subjects the synovium of the joint space extended 1 to 2 mm outside the boundaries of the joint in one or more locations. These synovial extensions, which could be considered to be small synovial cysts, maintained communication with the joint space, and were found on both the anterior and posterior aspects of the joint. Anteriorly the spaces most often extended along the posterior border of the ligamentum flavum (64% of Z joints). Sometimes a synovial joint extension extended directly into the ligamentum flavum (8% of cases). Posteriorly the synovial cysts usually extended either laterally along the superior articular process (7% of cases) or medially along the inferior articular process (29%). Extensions were found on both the inferior and superior articular processes in 41% of the Z joints, and no synovial extensions were found in 23% (7% of individuals) of the Z joints. Xu et al. (1991) believed that the synovial joint extensions (synovial cysts) probably were more common in the older population (e.g., the specimens in their study) than in younger age groups. They stated that their findings may explain why Z joint arthrography (visualization of the Z joint after injection with radiopaque dye) could be successful even when the joint space was not entered with the injecting needle (i.e., the needle could enter a synovial extension).


In another study, Xu, Haughton, and Carrera (1990) visualized the synovial joint extensions (cysts) with MRI. Their positive identification of these synovial joint extensions was aided with the injection of paramagnetic contrast medium (gadodiamide, Winthrop Pharmaceuticals). Their imaging was performed on dissected spines using small surface coils, long acquisition times, and thin slice thicknesses. Therefore clear delineation of these extensions is probably still beyond the resolving capabilities of MRI scans obtained in a typical clinical setting. However, Xu et al. (1991) thought their results helped to explain the variable appearance of the facet joints on MRI scans. They stated that “the inhomogeneity detected at MR imaging and computerized tomography in the ligamentum flavum near the facet joint most likely represents extension of the joint capsule between the ligamentum flavum and the articular processes. …” (Xu et al., 1991).


The superior and inferior recesses are filled with fibrofatty pads. These pads are well vascularized and are lined with a synovial membrane. They also protrude a significant distance into the superior and inferior aspects of the Z joint. Engel and Bogduk (1982) state that adipose tissue pads probably develop from undifferentiated mesenchyme of the embryologic Z joint. Furthermore, they note that in certain instances, mechanical stress to the joint may cause an adipose tissue pad to undergo fibrous metaplasia, which results in the formation of a large fibroadipose meniscoid (an adipose tissue pad with a fibrous tip composed of dense connective tissue). The authors believed that both the adipose tissue pads and the normally found synovial folds, or meniscoids, “play some form of normal functional role” (see Fig. 7-5).


In addition, “fringes” of synovium extend from the capsule to the region between the articular facets. These fringes fill the small region in which the facets do not completely come together.


Sometimes a fatty synovial fold develops a relatively long fibrous tip that extends a considerable distance between the joint surfaces, where it may become compressed (Taylor and Twomey, 1986). Such protruding synovial folds have been associated with the early stages of degeneration (Rauschning, 1987). Rauschning (1987) typically found hemarthrosis and effusion into the Z joints when the meniscal folds of this type were torn or “nipped” between the joint surfaces.


Occasionally a piece of articular cartilage breaks from the superior or inferior articular facet as humans age. The piece usually breaks along the posterior aspect of the Z joint, parallel to the joint space. However, the attachment to the articular capsule usually is maintained. The result is the presence of a large, fibrocartilaginous meniscoid inclusion within the joint. Taylor and Twomey (1986) reported that the formation of this type of meniscoid is partially caused by the regular pulling action on the posterior articular capsule by the multifidi muscles that originate from these capsules. The attachment of the capsule to the periphery of the articular cartilage may then result in the cartilage tears found to run parallel with the joint surface. Again, the torn cartilage fragment is capable of developing into a Z joint meniscoid, which can become interposed between the two surfaces of the joint. The authors also noted that the posterior aspect of the Z joint may open when the multifidi and other deep back muscles relax, allowing the meniscoids and other joint inclusions to bow into the joint space and become entrapped. The result of this type of entrapment could be (a) loss of motion (locked back), resulting from the cartilage being lodged between two opposing joint surfaces; (b) pain, because the meniscoids remain attached and therefore might put traction on the pain-sensitive joint capsule; or (c) both decreased motion and pain.


As described in Chapter 2, the Z joint articular capsule receives sensory innervation from the medial branch of the posterior primary division of three consecutive spinal nerves. Using nerve tracing techniques in rats, Suseki et al. (1997) found that some sensory neurons innervating the lower lumbar Z joint capsules arise from the L1 and L2 dorsal root ganglia. These sensory fibers course through the lumbar sympathetic chain and then through gray communicating rami to reach the lower lumbar Z joints. These authors felt that this innervation of lower lumbar spinal tissues by sensory nerves arising from upper lumbar dorsal root ganglia might help to explain the clinical finding that pathology of lower lumbar spinal tissues sometimes can be described by patients as referring to regions innervated by higher lumbar segments (e.g., radiation into the inguinal region from a painful L5-S1 Z joint).


The pain-sensitive articular capsule and the synovial lining of the ligamentum flavum of each lumbar Z joint normally are held out of the joint by three structures. First, the multifidus lumborum muscles take part of their origin (several originate from each vertebra) from the posterior aspect of each articular capsule (Taylor and Twomey, 1986

Jun 11, 2016 | Posted by in ANATOMY | Comments Off on The Lumbar Region
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